Figure 3

Data preprocessing

# loading functions
library(ggbeeswarm)
library(rstatix)
library(ggpubr)
library(wesanderson)
library(patchwork)
library(ggbreak)
library(gridExtra)
library(pheatmap)
library(scales)
library("readxl")
source("func.R")

Loading required package: ggplot2


Attaching package: 'rstatix'


The following object is masked from 'package:stats':

    filter


ggbreak v0.1.1

If you use ggbreak in published research, please cite the following
paper:

S Xu, M Chen, T Feng, L Zhan, L Zhou, G Yu. Use ggbreak to effectively
utilize plotting space to deal with large datasets and outliers.
Frontiers in Genetics. 2021, 12:774846. doi: 10.3389/fgene.2021.774846



Attaching package: 'ape'


The following object is masked from 'package:ggpubr':

    rotate


ggtree v3.7.2 For help: https://yulab-smu.top/treedata-book/

If you use the ggtree package suite in published research, please cite
the appropriate paper(s):

Guangchuang Yu, David Smith, Huachen Zhu, Yi Guan, Tommy Tsan-Yuk Lam.
ggtree: an R package for visualization and annotation of phylogenetic
trees with their covariates and other associated data. Methods in
Ecology and Evolution. 2017, 8(1):28-36. doi:10.1111/2041-210X.12628

S Xu, Z Dai, P Guo, X Fu, S Liu, L Zhou, W Tang, T Feng, M Chen, L
Zhan, T Wu, E Hu, Y Jiang, X Bo, G Yu. ggtreeExtra: Compact
visualization of richly annotated phylogenetic data. Molecular Biology
and Evolution. 2021, 38(9):4039-4042. doi: 10.1093/molbev/msab166

Shuangbin Xu, Lin Li, Xiao Luo, Meijun Chen, Wenli Tang, Li Zhan, Zehan
Dai, Tommy T. Lam, Yi Guan, Guangchuang Yu. Ggtree: A serialized data
object for visualization of a phylogenetic tree and annotation data.
iMeta 2022, 1(4):e56. doi:10.1002/imt2.56 


Attaching package: 'ggtree'


The following object is masked from 'package:ape':

    rotate


The following object is masked from 'package:ggpubr':

    rotate


Loading required package: maps


Attaching package: 'phytools'


The following object is masked from 'package:scales':

    rescale


-- Attaching core tidyverse packages ------------------------ tidyverse 2.0.0 --
v dplyr     1.1.1     v readr     2.1.4
v forcats   1.0.0     v stringr   1.5.0
v lubridate 1.9.2     v tibble    3.2.1
v purrr     1.0.1     v tidyr     1.3.0
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i Use the conflicted package (<http://conflicted.r-lib.org/>) to force all conflicts to become errors

Processing tables

l1_tbl <- read_tsv("../results/crc_pairwise_l1.tsv")
markerlengths <- read_tsv("../results/crc_markerlengths.tsv")
divergence_timing <- read_tsv("../results/crc_divergence_timing.tsv")
mrca_tbl <- read_tsv("../results/crc_mrca_table.tsv")

Rows: 3588 Columns: 6
-- Column specification --------------------------------------------------------
Delimiter: "\t"
chr (2): a, b
dbl (4): l1, r, marker, divs

i Use `spec()` to retrieve the full column specification for this data.
i Specify the column types or set `show_col_types = FALSE` to quiet this message.
Rows: 11683 Columns: 4
-- Column specification --------------------------------------------------------
Delimiter: "\t"
chr (3): sample, marker, subject
dbl (1): length

i Use `spec()` to retrieve the full column specification for this data.
i Specify the column types or set `show_col_types = FALSE` to quiet this message.
Rows: 656 Columns: 4
-- Column specification --------------------------------------------------------
Delimiter: "\t"
chr (3): samples, comparison, subject
dbl (1): mrca

i Use `spec()` to retrieve the full column specification for this data.
i Specify the column types or set `show_col_types = FALSE` to quiet this message.
Rows: 37 Columns: 3
-- Column specification --------------------------------------------------------
Delimiter: "\t"
chr (1): subject
dbl (2): all_mrca, ad_ad_mrca

i Use `spec()` to retrieve the full column specification for this data.
i Specify the column types or set `show_col_types = FALSE` to quiet this message.

normal_samples <- l1_tbl %>%
      mutate(
            subject = str_extract(a, "C[0-9]{1,3}"),
            sample_a = str_extract(a, "(?<=C[0-9]{1,3})[:alpha:][:digit:]*"),
            sample_b = str_extract(b, "(?<=C[0-9]{1,3})[:alpha:][:digit:]*"),
            type_a = str_extract(a, "(?<=C[0-9]{1,3})[:alpha:]"),
            type_b = str_extract(b, "(?<=C[0-9]{1,3})[:alpha:]"),
            suffix_a = str_extract(a, "[:lower:]$"),
            suffix_b = str_extract(b, "[:lower:]$")
      ) %>%
      group_by(subject) %>%
      filter(str_detect(a, "N") | str_detect(b, "N"), !(str_detect(a, "N") & str_detect(b, "N"))) %>%
      mutate(normal = ifelse(str_detect(a, "N"), a, b)) %>%
      select(subject, normal) %>%
      distinct() %>%
      dplyr::slice_head() %>% 
      pull(normal)

# select only the first normal sample
annotated_cmb_cell_divs <- l1_tbl %>%
      mutate(
            subject = str_extract(a, "C[0-9]{1,3}"),
            sample_a = str_extract(a, "(?<=C[0-9]{1,3})[:alpha:][:digit:]*"),
            sample_b = str_extract(b, "(?<=C[0-9]{1,3})[:alpha:][:digit:]*"),
            type_a = str_extract(a, "(?<=C[0-9]{1,3})[:alpha:]"),
            type_b = str_extract(b, "(?<=C[0-9]{1,3})[:alpha:]"),
            suffix_a = str_extract(a, "[:lower:]$"),
            suffix_b = str_extract(b, "[:lower:]$")
      ) %>%
      group_by(subject) %>%
            filter(
                  (!str_detect(a, "N") & !str_detect(b, "N")) |
                        (str_detect(a, "N", negate = TRUE) & (b %in% normal_samples)) |
                        (str_detect(b, "N", negate = TRUE) & (a %in% normal_samples))
            ) %>%
      ungroup()

# transform mrca table into format fo easier plotting 
long_mrca_tbl  <- mrca_tbl  %>% 
    pivot_longer(2:3, names_to="comparison", 
                values_to="mrca_divs") %>% 
     mutate(sample_type = case_when(
         comparison == "all_mrca" ~ "Whole Tumor",
         comparison == "ad_ad_mrca" ~ "Adenoma"
     ))

Defining MSI subjects by whether more than 10% of their mutations are deletion over 1bp:

msi_samples <- markerlengths %>%
    group_by(subject) %>%
    mutate(large_del = (length < (-1))) %>%
    count(large_del) %>%
    mutate(del_frac = n / sum(n)) %>%
    filter(large_del, del_frac > 0.1)
msi_samples
msi_tumors <- msi_samples$subject

A grouped_df: 6 x 4

subject	large_del	n	del_frac
<chr>	<lgl>	<int>	<dbl>
C102	TRUE	195	0.4987212
C12	TRUE	169	0.6627451
C38	TRUE	135	0.6108597
C6	TRUE	73	0.3160173
C92	TRUE	138	0.5307692
C95	TRUE	144	0.6153846

# ordering subjects from lowest to highest number
subjects <- as.list((markerlengths) %>%
    pull(subject) %>%
    unique()) %>%
    str_sort(numeric=TRUE)

markerlengths %>%
    filter(!(subject %in% msi_samples$subject)) %>% 
    group_by(subject) %>%
    summarize(length=mean(length)) %>% 
    summarize(mean(length))

A tibble: 1 x 1

mean(length)
<dbl>
-0.1030013

markerlengths %>%
    filter(!(subject %in% msi_samples$subject)) %>%
    group_by(subject) %>%
    mutate(deletion = length < 0) %>%
    count(deletion) %>%
    summarise(deletion_rate = n[deletion] / sum(n)) %>%
    summarise(mean(deletion_rate))

A tibble: 1 x 1

mean(deletion_rate)
<dbl>
0.565739

n_counts <- markerlengths %>%
    mutate(
        subject = fct_relevel(subject, subjects)
    ) %>% 
    group_by(subject) %>%
        count() %>%
        mutate(n=paste0("n=", n))

markerlengths %>%
    ungroup() %>%
    mutate(
        MSI = ifelse(subject %in% msi_samples$subject, TRUE, FALSE),
        subject = fct_relevel(subject, subjects)
    ) %>% 
    ggplot(aes(subject, length)) +
    geom_quasirandom(aes(color = MSI), width=0.3) +
    geom_boxplot(alpha = 0) +
    geom_text(data=n_counts, aes(y=-10, label=n), angle=90, size=10) +
    coord_cartesian(ylim=c(-10.3, NA)) +
    scale_y_continuous(breaks = seq(-10, 10, 2)) +
    scale_color_manual(
        values = c(wes_palette("Zissou1")[1], wes_palette("Zissou1")[5]),
        name = "MMR Status",
        labels = c("MMRp", "MMRd")
    ) +
    labs(y = "Polyguanine mean length") +
    theme_martin() +
    theme(
            axis.title.x = element_blank(), axis.text.x = element_text(angle = 45, hjust = 1),
            panel.grid.major.y = element_line(linewidth = 1, color = "grey82", linetype = 3),
            panel.grid.minor.y = element_line(linewidth = 1, color = "grey82", linetype = 3),
            legend.key.height = unit(20, "pt"), legend.key.width = unit(20, "pt"), 
            legend.text = element_text(size = 28), legend.title = element_text(size=28)
      ) +
    guides(colour = guide_legend(override.aes = list(size=12)))
ggsave("../plots/Figure3/Extended_Data_Fig10a.pdf", height=11, width=24)

Figure 3A

subject_i <- "C31"
c31_tree <- plot_tree(subject_i, l1_tbl)
subject_ggtree <- ggtree(c31_tree, size = 1.5) +
    theme_tree2() +
    labs(
      x = "Divisions from zygote"
    ) 

   # maximum y dimension for plotting
  max.y <- max(subject_ggtree$data$y)+1
  
  # maximum x dimension for plotting
  max.x <- max(subject_ggtree$data$x)*1.1
  
  # annotating the sample type
  subject_ggtree$data <- subject_ggtree$data %>%
      mutate(
          type = str_extract(label, "(?<=C[0-9]{1,3})[:alpha:]"),
          label = str_remove(label, subject_i)
      )
  subject_ggtree +
      # annotate primary tumor diversification
      annotate("rect", xmin = 1400, xmax = 2050, ymin = 1, ymax = 7.5, alpha = .2, fill = "firebrick2") +
      annotate("text", x = 1600, y = 9.5, label = "Primary tumor\ndiversification", color = "firebrick2", size = 12) +
      # annotate MRCA
      geom_nodepoint(data = . %>% filter(node == 29), size = 12, color = "grey42") +
      annotate("text", x = 1300, y = 2, label = "MRCA", color = "grey42", size = 12) +
      # annotate trunk
      annotate("text", x = 500, y = 4, label = "{", color = "blue3", size = 72, angle=90) +
      annotate("text", x = 600, y = 5.5, label = "Trunk", color = "blue3", size = 12) +
      # annotate metastasis divergence
      geom_nodepoint(data = . %>% filter(node == 24), size = 12, color = "orange2") +
      annotate("text", x = 2100, y = 11, label = "Metastasis\ndivergence", color = "orange2", size = 12) +
      # rest of the tree
      geom_tiplab(aes(color = type), size = 11, ) +
      scale_color_manual(
          values = c(A = "purple2", L = "darkgreen", M = "orange2", N = "grey23", P = "firebrick2"),
          guide = "none"
      ) +
    theme(
        axis.line.x = element_line(linewidth = 1.5),
        axis.title.x = element_text(size = 35, color = "black"),
        axis.text.x = element_text(size = 35, color = "black"),
        axis.ticks.x = element_line(color = "black", linewidth = 1),
        axis.ticks.length.x = unit(0.2, "cm"), plot.title = element_text(size = 35),
        axis.line.y = element_blank(),
        axis.title.y = element_blank(),
        axis.text.y = element_blank(),
        axis.ticks.y = element_blank()
    ) +
    xlim(0, max.x) +
    scale_y_reverse()

ggsave("../plots/Figure3/Fig3A.pdf", height=11, width=15)

Scale for y is already present.
Adding another scale for y, which will replace the existing scale.

Cell division timing

Loading in clinical data

natgen_age <- read_xlsx("../data/Reiter_2020_Supplementary_Tables.xlsx", sheet=3,
                skip=1)  %>% 
    rename(subject = 2, age = 4, size = 16) %>%
    select(subject, age, size) %>%
    mutate(age = parse_number(age))

New names:
* `` -> `...1`

science_age <-  read_xlsx("../data/Naxerova_2017_patient_information.xlsx") %>%
     rename(subject = Patient, size=`Tumor size`, age=`Age at dianosis`) %>%
     select(subject, age, size) %>% 
     filter(subject!="C57")

clinical_tbl <- bind_rows(science_age, natgen_age)

crc_l1_clinical <- l1_tbl %>%
    mutate(subject = str_extract(a, "C[0-9]{1,3}")) %>%
    left_join(clinical_tbl) 

crc_mrca_clinical <- mrca_tbl %>%
    select(subject, all_mrca, ad_ad_mrca) %>%
    pivot_longer(2:3, names_to = "tumor", values_to = "divs") %>% 
    left_join(clinical_tbl)

Joining with `by = join_by(subject)`
Joining with `by = join_by(subject)`

Plotting MRCA divisions of cancers and adenomas:

crc_mrca_clinical %>%
    filter((!subject %in% msi_tumors)) %>%
    ggplot(aes(tumor, divs)) +
    geom_beeswarm(aes(fill = tumor), shape=21, cex = 4.8, size = 9, color = "grey23", stroke = 1) +
    scale_fill_manual(labels=c("Adenoma", "Colorectal\ncancer"), values = c("purple2", "firebrick2"))  +
    geom_boxplot(alpha = 0, size = 1, color = "grey23") +
    scale_x_discrete(labels=c("Adenoma", "Colorectal\ncancer")) +
    labs(y="Divisions from zygote to tumor MRCA") +
    theme_martin() +
    theme(axis.title.x = element_blank(),
    legend.title = element_blank(), legend.text = element_text(size=20), legend.position = c(0.2, 0.8))
ggsave("../plots/Figure3/Fig3B.pdf", height=11, width=8)

Warning message:
"A numeric `legend.position` argument in `theme()` was deprecated in ggplot2
3.5.0.
i Please use the `legend.position.inside` argument of `theme()` instead."
Warning message:
"Removed 28 rows containing non-finite outside the scale range
(`stat_boxplot()`)."
Warning message:
"Removed 28 rows containing missing values or values outside the scale range
(`geom_point()`)."
Warning message:
"Removed 28 rows containing non-finite outside the scale range
(`stat_boxplot()`)."
Warning message:
"Removed 28 rows containing missing values or values outside the scale range
(`geom_point()`)."

N for each boxplot

crc_mrca_clinical %>%
    filter((!subject %in% msi_tumors), !is.na(divs)) %>%
    group_by(tumor) %>%
    count()

A grouped_df: 2 x 2

tumor	n
<chr>	<int>
ad_ad_mrca	3
all_mrca	31

Plotting age and divisions to MRCA:

crc_mrca_clinical %>%
    filter(!(subject %in% msi_tumors)) %>%
    ggplot(aes(age, divs)) +
    geom_smooth(data = . %>% filter(tumor != "ad_ad_mrca"), method = "lm", size = 2, alpha = 0.2, color = "grey23") +
    geom_point(aes(fill = tumor), size = 9, pch = 21, stroke = 1) +
    scale_fill_manual(labels=c("Adenoma", "Colorectal\ncancer"), values = c("purple2", "firebrick2"))  +
    stat_cor(data=.%>% filter(tumor!="ad_ad_mrca"), size = 10, p.accuracy = 10e-4) +
    labs(x="Age", y="Divisions from zygote to tumor MRCA") +
    theme_martin() +
    theme(legend.title = element_blank(), legend.text = element_text(size=20), legend.position = c(0.1, 0.8))
ggsave("../plots/Figure3/Fig3C.pdf", height=11, width=14)

`geom_smooth()` using formula = 'y ~ x'
Warning message:
"Removed 28 rows containing missing values or values outside the scale range
(`geom_point()`)."
`geom_smooth()` using formula = 'y ~ x'
Warning message:
"Removed 28 rows containing missing values or values outside the scale range
(`geom_point()`)."

Processing data from intestinal stem cell colonies

Markerlengths for the ISC colonies:

# directory of the results the colon ISCs used in Naxerova et al 2017.
dir_list <- list.files("../data/colon_iscs",
    pattern = "_R$", full.names = TRUE
)

l <- map(dir_list, get_markerlengths)
markerlengths_isc_raw  <- bind_rows(l)

P1947

STE0071

STE0072

STE0074

STE0076

Distance from the root needs to be subtracted manually, as the blood or bulk samples represent the germline genotype:

markerlengths_isc <- markerlengths_isc_raw %>%
    mutate(sample=str_sub(sample, end=-3)) %>% 
    group_by(subject, marker) %>%
    filter(any(str_detect(sample, "B"))) %>% 
    mutate(length = length - length[sample==str_subset(sample, "B")[1]]) %>% 
    ungroup

Getting the minimum number of marker all samples agree on, as long as that's more than 70% of the maximum possible markers

get_minimum_marker_table  <- function(subject_i, markerlengths){

marker_tbl <-  markerlengths  %>% 
    filter(subject==subject_i)  %>% 
    group_by(sample)  %>% 
    add_count(sample)  %>% 
    ungroup()  %>% 
    mutate(minimum_markers = max(n)*0.7) %>% 
    filter(n>minimum_markers)  

samples <- unique(marker_tbl$sample)
marker_list <- lapply(samples, get_sampler_marker, marker_tbl)

common_markers  <- Reduce(intersect, marker_list)
n_common_markers  <- length(common_markers)

markerlengths %>%
    filter(subject == subject_i, marker %in% common_markers) %>%
    group_by(sample) %>%
    add_count(sample) %>%
    filter(n == n_common_markers) %>%
    select(-n) %>%
    mutate(markers=n_common_markers)
    
    }

# function to get markers that are present in all samples
get_sampler_marker  <- function(sample_i, marker_tbl) {

    marker_tbl  %>% 
    filter(sample==sample_i)  %>% 
    pull(marker)  %>% 
    unique()
}

# removing all markers that didn't amplify in 70% of the cases
subjects  <- unique(markerlengths_isc$subject)
minimum_marker_tbls  <- lapply(subjects, get_minimum_marker_table, markerlengths_isc)

Saving heatmaps with patient ages

create_heatmap_isc <- function(mean_lengths) {
    
    subject_i <- unique(mean_lengths$subject)

    age <-  case_when(
        str_detect(subject_i, "STE0071") ~ 4, str_detect(subject_i, "STE0072") ~ 4,
        str_detect(subject_i, "STE0076") ~ 9, str_detect(subject_i, "STE0074")~14, str_detect(subject_i, "P1947")~66
    ) 
    
    filtered_matrix <- mean_lengths %>% 
        mutate(sample = str_remove_all(sample, paste0(subject_i, "-"))) %>% 
        ungroup() %>% 
        select(-subject) %>% 
        pivot_wider(names_from = marker, 
        values_from = length) %>% 
        column_to_rownames("sample") %>%
        as.matrix()
    
    minmax <- max(abs(filtered_matrix), na.rm = TRUE)
    
    plot_title <- paste0("Donor: ", subject_i, " (", age, " years old)")

    hm <- pheatmap::pheatmap(filtered_matrix, clustering_distance_rows = "manhattan", 
        clustering_distance_cols = "manhattan", 
        display_numbers = TRUE, number_color = "black", fontsize = 6, 
        color = colorRampPalette(c("seagreen", "white", "purple3"))(42), 
        na_col = "yellow", breaks = seq(-minmax, minmax, length.out = 43), 
        silent = TRUE, main=plot_title)

    ggsave(paste0("../plots/Supplementary_figures/isc_hm/", subject_i, "_heatmap.pdf"), 
        hm, width = 10, height = 4)

}

isc_hm_tbls <- minimum_marker_tbls %>%
    map(\(x) select(x, -markers))

walk(isc_hm_tbls, create_heatmap_isc)

Calculating L1 distance and cell divisions

Creating function to go through each sample separately

l1_cell_divs <- function(tbl) {
# find samples
samples <- tbl$sample %>% unique

combos_wide <- combn(samples, m= 2) %>% as.data.frame()

## make combo table longer
combos_long <- data.frame(a=as.character(combos_wide[1,]), b=as.character(combos_wide[2,]))

## only use combintions from the same subject
combos <- combos_long 
    
# getting l1 for all intrapatient sample combinations in the cohort
l1 <- lapply(1:nrow(combos), get_l1_r_for_combination, combos, tbl)

bind_rows(l1) %>%
    mutate(divs = l1 / 9.43139014888478e-05)
}

isc_divs_tbll1 <- map(minimum_marker_tbls, l1_cell_divs) %>%
    bind_rows()

Manually annotating from supplementary information of Naxerova et al 2017.

isc_l1 <- isc_divs_tbll1 %>%
    mutate(age = case_when(
        str_detect(a, "STE0071") ~ 4, str_detect(a, "STE0072") ~ 4,
        str_detect(a, "STE0076") ~ 9, str_detect(a, "STE0074")~14, str_detect(a, "P1947")~66
    ), age=age+0.75) %>% 
    filter(str_detect(a, "B")|str_detect(b, "B")) %>% 
    separate(a, c("subject", NA), "-") %>%
    select(subject, divs, age) %>%
    mutate(group="isc")

Plotting days per division:

df_divs_stats <- crc_mrca_clinical %>%
  filter(!(subject %in% msi_tumors)) %>%
  filter(tumor=="all_mrca") %>% 
  select(subject, divs, age) %>%
  mutate(age=age+0.75-5, group="all_mrca") %>% 
  bind_rows(isc_l1) %>%
  drop_na() %>%
  mutate(divs_per_year=divs/age)  %>% 
  mutate(days_per_divs=365/divs_per_year)  %>%  
  filter(!is.na(days_per_divs))  %>% 
  group_by(group) %>% 
  mutate(
    n = n(),
    median = median(days_per_divs),
    mean = mean(days_per_divs),
    max = max(days_per_divs)
  ) %>% 
  ungroup() %>% 
  mutate(group = fct_relevel(group, "all_mrca", "isc"),
  group_num = as.numeric(fct_rev(group)))

options(repr.plot.width=10, repr.plot.height=7)

ggplot(df_divs_stats, aes(days_per_divs, group_num, color = group)) +
  stat_summary(
    geom = "linerange",
    fun.min = function(x) -Inf,
    fun.max = function(x) median(x, na.rm = TRUE),
    linetype = "dotted",
    orientation = "y",
    size = .7
  ) +
  geom_point(
    aes(y = group_num - .15), 
    shape = "|",
    size = 5,
    alpha = .33
  ) +
  ggdist::stat_halfeye(
    aes(
      y = group_num,
      color = group,
      fill = after_scale(colorspace::lighten(color, .3))
    ),
    size=3,
    stroke=2,
    shape = 1,
    height = 0.8,
    point_size = 3,
    interval_size = 1.8,
    adjust = .59,
    .width = c(0, 1)
  )  +
  geom_text(
    aes(x = median, label = format(round(median, 2), nsmall = 2)),
    stat = "unique",
    color = "white",
    family = "Helvetica",
    fontface = "bold",
    size = 12,
    nudge_y = .12,
  ) +
  geom_text(
    aes(x = max, label = glue::glue("n = {n}")),
    stat = "unique",
    family = "Helvetica",
    fontface = "bold",
    size = 12,
    hjust = 0,
    nudge_x = 5,
    nudge_y = .02
  )  +
  coord_cartesian(clip = "off", expand = TRUE) +
  scale_y_continuous(
    limits = c(.55, NA),
    breaks = 1:2,
    labels = c("Zygote to\nintestinal\nstem\ncells", "Zygote to\ncolorectal\ncancer\nMRCA"),
  )  +
  scale_color_manual(values = c("all_mrca"="firebrick2", "isc"=wes_palette("Royal1")[1]),
                       guide="none") +
  scale_fill_manual(values = c("all_mrca"="firebrick2", "isc"=wes_palette("Royal1")[1]),
                       guide="none") +
  theme_martin() +
  coord_trans(x = "log2") +
  scale_x_continuous(breaks = breaks_log(8, base=2), expand = expansion(mult = 0, add = c(0.3, 0.75))) + 
  theme(
    panel.grid.major.x = element_line(size = .35),
    panel.grid.major.y = element_blank()
    ) +
    labs(x = "Days per division", y = "")
ggsave("../plots/Figure3/Fig3D.pdf", height=11, width=19)

Coordinate system already present. Adding new coordinate system, which will
replace the existing one.

How often do samples divide after tumor initation?

science_cohort_timing <- read_excel("../data/Reiter_2020_Supplementary_Tables.xlsx", sheet = 1, skip = 1) %>%
    select(Patient, `Treatment between primary and distant metastasis resections`) %>%
    rename(subject = 1, timing = 2) %>%
    mutate(timing = ifelse(timing == "YES", "metachronous", "synchronous"))

natgent_cohort_timing <- read_excel("../data/Reiter_2020_Supplementary_Tables.xlsx", sheet = 3, skip = 1) %>%
    select(2, `Metachronous or synchronous (0-6 months) distant metastasis?`) %>%
    rename(subject = 1, timing = 2) %>%
    #C90 was manually reviewed to be synchronous
    mutate(timing=ifelse(subject=="C90", "synchronous", timing))

timing_tbl <- bind_rows(science_cohort_timing, natgent_cohort_timing) %>%
    drop_na()

meta_subjects <- timing_tbl %>%
    filter(timing == "metachronous") %>%
    pull(subject)

New names:
* `` -> `...1`
* `` -> `...12`
New names:
* `` -> `...1`

Fig. 3E

Showing the time from cancer initation to each sample type:

tumor_ad_mrca <- long_mrca_tbl %>%
    select(-sample_type) %>% 
    filter(comparison == "all_mrca" | comparison == "ad_ad_mrca") %>%
    pivot_wider(names_from = "comparison", values_from="mrca_divs") %>% 
    rename(mrca_divs=all_mrca, ad_divs=ad_ad_mrca)

plot_divs_from_mrca <- tumor_ad_mrca %>%
       left_join(annotated_cmb_cell_divs) %>%
       group_by(subject) %>%
       filter((str_detect(a, "N") | str_detect(b, "N"))) %>%
       ungroup() %>%
       mutate(
              divs_from_mrca = ifelse(str_detect(a, "A") | str_detect(b, "A"), divs - ad_divs, divs - mrca_divs),
              sample_type = ifelse(type_a == "N", type_b, type_a)
       ) %>%
    filter(!((subject %in% meta_subjects) & sample_type == "M")) %>%
    mutate(sample_type = fct_relevel(sample_type, "A", "P", "L", "M"))

Joining with `by = join_by(subject)`

Kruskal Wallis test across all groups.

plot_divs_from_mrca %>%
    kruskal_test(divs_from_mrca ~ sample_type)

A rstatix_test: 1 x 6

	.y.	n	statistic	df	p	method
	<chr>	<int>	<dbl>	<int>	<dbl>	<chr>
1	divs_from_mrca	399	31.73624	3	5.95e-07	Kruskal-Wallis

mrca_divs_pp <- plot_divs_from_mrca %>%
    filter(sample_type %in% c("A", "P")) %>%
    dunn_test(divs_from_mrca ~ sample_type) 

mrca_divs_lp <- plot_divs_from_mrca %>%
    filter(sample_type %in% c("L", "P")) %>%
    dunn_test(divs_from_mrca ~ sample_type) 

mrca_divs_mp <- plot_divs_from_mrca %>%
    filter(sample_type %in% c("M", "P")) %>%
    dunn_test(divs_from_mrca ~ sample_type) 

mrca_divs_p <- bind_rows(mrca_divs_pp, mrca_divs_lp, mrca_divs_mp) %>%
    mutate(group1 = fct_relevel(group1, "A", "P", "L", "M")) %>%
    adjust_pvalue() %>%
    add_xy_position(x = "sample_type") %>%
    p_format(accuracy = 1e-20, add.p = TRUE, digits = 3) %>% 
    mutate(
        xmax = case_when(group2 == "L" ~ 3, group2 == "M" ~ 4, TRUE ~ xmax),
        y.position	 = case_when(group2 == "L" ~ 5968.966, group2 == "M" ~ 6468.966, TRUE ~ y.position)
    )

Warning message:
"There was 1 warning in `mutate()`.
i In argument: `group1 = fct_relevel(group1, "A", "P", "L", "M")`.
Caused by warning:
! 2 unknown levels in `f`: L and M"

plot_divs_from_mrca %>%
    ggplot(aes(sample_type, divs_from_mrca)) +
    geom_quasirandom(aes(fill = sample_type), width = 0.3, size = 9, pch = 21, color = "grey23", stroke = 1) +
    geom_boxplot(alpha=0, size=1, color="grey23") +
    scale_fill_manual(values = c("A"="purple2", "L"="darkgreen", 
                                  "M"="orange2", "N"="grey23", "P"="firebrick2"),
                       guide="none") +
    stat_pvalue_manual(mrca_divs_p, label = "p.adj", tip.length = 0.03, step.increase = 0.01, size = 10, bracket.size = 1) +
    scale_x_discrete(labels=c("Adenoma", "Primary \ntumor", "Lymph node\nmetastasis", "Distant\nmetastasis")) +
    coord_cartesian(ylim=c(0,7000)) +
    labs(y="Divisions from tumor MRCA to sample") +
    theme_martin() +
    theme(axis.title.x = element_blank())

ggsave("../plots/Figure3/Fig3E.pdf", width=19, height=11)

Warning message:
"Removed 4 rows containing non-finite outside the scale range
(`stat_boxplot()`)."
Warning message:
"Removed 4 rows containing missing values or values outside the scale range."
Warning message:
"Removed 4 rows containing non-finite outside the scale range
(`stat_boxplot()`)."
Warning message:
"Removed 4 rows containing missing values or values outside the scale range."

Extended Data Figure 6b

msi_subjects <- msi_samples$subject

plot_divs_from_mrca_ms <- plot_divs_from_mrca %>%
    filter(sample_type != "A") %>%
    mutate(
        sample_type = ifelse(subject %in% msi_subjects, paste0(sample_type, "_msi"), paste0(sample_type, "_mss")),
        sample_type = fct_relevel(sample_type, "P_mss", "P_msi", "L_mss", "L_msi", "M_mss", "M_msi")
    )

mrca_divs_lp_ms <- paste0("p=", wilcox.test(
    plot_divs_from_mrca_ms[plot_divs_from_mrca_ms$sample_type == "L_msi", ]$divs_from_mrca,
    plot_divs_from_mrca_ms[plot_divs_from_mrca_ms$sample_type == "L_mss", ]$divs_from_mrca
)$p.value %>% 
round(3))

mrca_divs_pp_ms <- paste0("p=", wilcox.test(
    plot_divs_from_mrca_ms[plot_divs_from_mrca_ms$sample_type == "P_msi", ]$divs_from_mrca,
    plot_divs_from_mrca_ms[plot_divs_from_mrca_ms$sample_type == "P_mss", ]$divs_from_mrca
)$p.value %>% 
round(3))

mrca_divs_mp_ms <- paste0("p=", wilcox.test(
    plot_divs_from_mrca_ms[plot_divs_from_mrca_ms$sample_type == "M_msi", ]$divs_from_mrca,
    plot_divs_from_mrca_ms[plot_divs_from_mrca_ms$sample_type == "M_mss", ]$divs_from_mrca
)$p.value %>% 
round(3))

options(repr.plot.width=18, repr.plot.height=7)


plot_divs_from_mrca_ms %>% 
    ggplot(aes(sample_type, divs_from_mrca)) +
    geom_quasirandom(aes(fill = sample_type), width = 0.3, size = 9, pch = 21, color = "grey23", stroke = 1) +
    geom_boxplot(alpha=0, size=1, color="grey23") +
    scale_fill_manual(values = c("A_mss"="purple2", "L_mss"="darkgreen", "L_msi"="green4", 
                                  "M_mss"="orange2", "M_msi"="orange1", "P_mss"="firebrick2", "P_msi"="firebrick1"),
                       guide="none") +
    geom_bracket(label=mrca_divs_lp_ms, y.position =5800,  xmin="L_mss", xmax="L_msi", tip.length = 0.03, vjust = -0.2, size = 1.5, label.size = 8) +
    geom_bracket(label=mrca_divs_pp_ms, y.position =5800,  xmin="P_mss", xmax="P_msi", tip.length = 0.03, vjust = -0.2, size = 1.5, label.size = 8) +
    geom_bracket(label=mrca_divs_mp_ms, y.position =5800,  xmin="M_mss", xmax="M_msi", tip.length = 0.03, vjust = -0.2, size = 1.5, label.size = 8) +
    scale_x_discrete(labels=c("Primary \ntumor\n(MMRp)", "Primary \ntumor\n(MMRd)", 
                                "Lymph node\nmetastasis\n(MMRp)", "Lymph node\nmetastasis\n(MMRd)", 
                                "Distant\nmetastasis\n(MMRp)", "Distant\nmetastasis\n(MMRd)")) +
    coord_cartesian(ylim = c(0, 6000)) +
        labs(y = "Divisions from tumor\nMRCA to sample") +
        theme_martin() +
        theme(axis.title.x = element_blank(), axis.text.x = element_text(size=20))
    ggsave("../plots/Figure3/Extended_Data_Fig6b.pdf", width=14)

Saving 14 x 7 in image

plot_divs_from_mrca_ms %>%
    count(sample_type)

A tibble: 6 x 2

sample_type	n
<fct>	<int>
P_mss	150
P_msi	33
L_mss	106
L_msi	24
M_mss	65
M_msi	4

Extended Data Figure 6c

cr_intersample <- annotated_cmb_cell_divs %>%
    filter(type_a == "P" | type_b == "P") %>%
    mutate(sample_type = case_when(type_a == "P" & type_b == "P" ~ "P", type_a == "M" | type_b == "M" ~ "M", type_a == "L" | type_b == "L" ~ "L")) %>%
    filter(!is.na(sample_type), !(subject %in% meta_subjects)) %>% 
    mutate(sample_type = fct_relevel(sample_type, "P", "L", "M")) %>% 
    group_by(subject) %>%
    mutate(pt_pt_r = mean(r[sample_type == "P"])) %>%
    mutate(r=r/pt_pt_r) %>% 
    ungroup()

cr_intersample_lp <- cr_intersample %>%
    filter(sample_type %in% c("L", "P")) %>%
    dunn_test(r ~ sample_type) 

cr_intersample_mp <- cr_intersample %>%
    filter(sample_type %in% c("M", "P")) %>%
    dunn_test(r ~ sample_type) 

cr_intersample_lm <- cr_intersample %>%
    filter(sample_type %in% c("L", "M")) %>%
        mutate(sample_type = fct_relevel(sample_type, "L", "M")) %>%

    dunn_test(r ~ sample_type) 

cr_intersample_p <- bind_rows(cr_intersample_lp, cr_intersample_mp, cr_intersample_lm) %>%
    mutate(group2 = fct_relevel(group2, "L", "M")) %>%
    adjust_pvalue() %>%
    add_xy_position(x = "sample_type")  %>% 
    p_format(accuracy = 1e-03, add.p = TRUE, digits = 2) %>%
    mutate(
        xmax = case_when(group2 == "M" ~ 3, TRUE ~ xmax),
        y.position	 = case_when( group2 == "M" & group1 == "L" ~ 1.2, group2 == "M" ~ 1.1, TRUE ~ y.position)
    )

cr_intersample_lm<- annotated_cmb_cell_divs %>%
    filter(type_a == "P" | type_b == "P") %>%
    mutate(sample_type = case_when(type_a == "P" & type_b == "P" ~ "P", type_a == "M" | type_b == "M" ~ "M", type_a == "L" | type_b == "L" ~ "L")) %>%
    filter(!is.na(sample_type), !(subject %in% meta_subjects)) %>%
    mutate(sample_type = fct_relevel(sample_type, "P", "L", "M")) %>%
    group_by(subject) %>%
    mutate(pt_pt_r = median(r[sample_type == "P"])) %>%
    mutate(r = log2((1 - r) / (1 - pt_pt_r))) %>%
    ungroup()

lm_p <- cr_intersample_lm %>%
    filter(sample_type %in% c("L", "M")) %>%
    mutate(sample_type = fct_relevel(sample_type, "L", "M")) %>%
    wilcox_test(r ~ sample_type)  %>% 
    add_xy_position(x = "sample_type") %>% 
    p_format(accuracy = 1e-03, add.p = TRUE, digits = 1) %>% 
    mutate(xmin=2,xmax=3)

cr_intersample_lm %>%
    #filter(sample_type != "P") %>%
    #group_by(sample_type, subject) %>%
    #summarize(r=mean(r)) %>% 
    ggplot(aes(sample_type, r)) +
    geom_quasirandom(aes(fill = sample_type), width = 0.3, size = 9, pch = 21, color = "grey23", stroke = 1) +
    geom_boxplot(alpha = 0, size = 1, color = "grey23")  +
    scale_fill_manual(
        values = c(
            "A" = "purple2", "L" = "darkgreen",
            "M" = "orange2", "N" = "grey23", "P" = "firebrick2"
        ),
        guide = "none"
    ) +
    stat_pvalue_manual(lm_p, tip.length = 0.03,  y.position = 5.2,
        step.increase = 0.0, size = 10, bracket.size = 1, bracket.nudge.y=0.2) +
    scale_x_discrete(labels = c("Primary\ntumor", "Lymph node\nmetastasis", "Distant\nmetastasis")) +
        coord_cartesian(ylim = c(-6, 6)) +
        labs(y = "Purity independent distance\nto primary tumor (normalized)") +
        theme_martin() +
        theme(axis.title.x = element_blank())
ggsave("../plots/Figure3/Extended_Data_Fig6c.pdf", height = 11, width = 11)

cr_intersample_lm %>%
    count(sample_type)

A tibble: 3 x 2

sample_type	n
<fct>	<int>
P	397
L	526
M	383

Fig 3F

Plotting individual trees

subject_i <- "C57"
tree <- plot_tree(subject_i, l1_tbl)
subject_ggtree <- ggtree(tree, size = 1.5) +
    theme_tree2() +
    labs(
      x = "Divisions from zygote"
    ) 

   # maximum y dimension for plotting
  max.y <- max(subject_ggtree$data$y)+1
  
  # maximum x dimension for plotting
  max.x <- max(subject_ggtree$data$x)*1.1
  
  # annotating the sample type
  subject_ggtree$data <- subject_ggtree$data %>%
      mutate(
          type = str_extract(label, "(?<=C[0-9]{1,3})[:alpha:]"),
          label = str_remove(label, subject_i)
      )
  
  subject_ggtree +
      geom_tiplab(aes(color = type), size = 11,  hjust = 0, shape = 21, fontface = 2) +
      scale_color_manual(
          values = c(A = "purple2", L = "darkgreen", M = "orange2", N = "grey23", P = "firebrick2"),
          guide = "none"
      ) +
    #geom_nodepoint(data=.%>% filter(node%in%c(13)), size=12,  fill="orange2", color="orange2") +
        theme(
            axis.line.x = element_line(linewidth = 1.5),
            axis.title.x = element_text(size = 35, color = "black"),
            axis.text.x = element_text(size = 35, color = "black"),
            axis.ticks.x = element_line(color = "black", linewidth = 1),
            axis.ticks.length.x = unit(0.2, "cm"), plot.title = element_text(size = 35),
            axis.line.y = element_blank(),
            axis.title.y = element_blank(),
            axis.text.y = element_blank(),
            axis.ticks.y = element_blank()
        ) +
        xlim(0, max.x)

ggsave("../plots/Figure3/Fig3F.pdf", height=11, width=11)

subject_i <- "C100"
tree <- plot_tree(subject_i, l1_tbl)
subject_ggtree <- ggtree(tree, size = 1.5) +
    theme_tree2() +
    labs(
      x = "Divisions from zygote"
    ) 

   # maximum y dimension for plotting
  max.y <- max(subject_ggtree$data$y)+1
  
  # maximum x dimension for plotting
  max.x <- max(subject_ggtree$data$x)*1.1
  
  # annotating the sample type
  subject_ggtree$data <- subject_ggtree$data %>%
      mutate(
          type = str_extract(label, "(?<=C[0-9]{1,3})[:alpha:]"),
          label = str_remove(label, subject_i),
      )
  
  subject_ggtree +
      #geom_tippoint(aes(color = type), color = "grey23", size = 11, nudge_x = -50, nudge_y = 0.2, angle = 45, hjust = 1, shape = 21, stroke = 1) +
      geom_tiplab(aes(color = type), size = 11,  hjust = 0, shape = 21, fontface = 2) +
      scale_color_manual(
          values = c(A = "purple2", L = "darkgreen", M = "orange2", N = "grey23", P = "firebrick2"),
          guide = "none"
      ) +
        geom_nodepoint(data = . %>% filter(node %in% c(29)), size = 12,  fill = "orange2", color = "orange2") +
        theme(
            axis.line.x = element_line(linewidth = 1.5),
            axis.title.x = element_text(size = 35, color = "black"),
            axis.text.x = element_text(size = 35, color = "black"),
            axis.ticks.x = element_line(color = "black", linewidth = 1),
            axis.ticks.length.x = unit(0.2, "cm"), plot.title = element_text(size = 35),
            axis.line.y = element_blank(),
            axis.title.y = element_blank(),
            axis.text.y = element_blank(),
            axis.ticks.y = element_blank()
        ) +
        xlim(0, max.x)

ggsave("../plots/Figure3/Fig3G.pdf", height=11, width=11)

Figure 3H

Metastasis private branches

# mrca of all samples
patient_mrca <- long_mrca_tbl %>%
    filter(comparison == "all_mrca") %>%
    select(-sample_type) %>%
    rename(divs = mrca_divs)

mrca_join_divg <- patient_mrca %>%
    select(-comparison) %>%
    rename(divs_to_mrca = divs)

# met divergence divisions 
met_sampled_div <- divergence_timing %>%
    filter(comparison == "met_primary") %>%
    mutate(sample_a = str_remove(samples, subject)) %>%
    select(-comparison) %>%
    rename(divs_to_divergence=mrca)

divs_from_divg_dm <- annotated_cmb_cell_divs %>%
    filter((str_detect(a, "N") & !str_detect(b, "N")) | (str_detect(b, "N") & !str_detect(a, "N"))) %>%
    mutate(comparison = ifelse(type_a == "N", type_b, type_a), sample_a = ifelse(str_detect(sample_a, "N"), sample_b, sample_a)) %>%
    left_join(met_sampled_div) %>%
    group_by(subject, comparison) %>% 
    left_join(mrca_join_divg) %>%
    mutate(
        across(c(divs, divs_to_divergence), ~ .x - divs_to_mrca), divs_after_divergence = divs-divs_to_divergence,
        fraction_to_divg = divs_to_divergence/divs
    ) %>% 
    mutate(divs = median(divs), divs_to_divergence = median(divs_to_divergence)) %>%
        filter(comparison %in% c("M", "P")) %>%
        group_by(subject) %>%
        fill(divs_to_divergence, .direction = "updown") %>%
        mutate(divs_after_divergence = divs - divs_to_divergence) %>%
        select(subject, divs_after_divergence, comparison) %>%
        distinct() %>%
        add_count() %>%
        filter(n == 2, !(subject %in% meta_subjects)) %>%
    mutate(comparison = fct_relevel(comparison, "P", "M"))

Joining with `by = join_by(subject, sample_a)`
Joining with `by = join_by(subject)`

divs_from_divg_dm %>%
    ungroup() %>%
    wilcox_test(divs_after_divergence ~ comparison, paired = T) %>%
    mutate(p=format(p, scientific=T)) %>% 
    add_xy_position(x = "comparison") %>%
    mutate(y.position = y.position+50, p=paste0("p=", p))

A rstatix_test: 1 x 11

.y.	group1	group2	n1	n2	statistic	p	y.position	groups	xmin	xmax
<chr>	<chr>	<chr>	<int>	<int>	<dbl>	<chr>	<dbl>	<named list>	<dbl>	<dbl>
divs_after_divergence	P	M	19	19	10	p=1.64e-04	1429.877	P, M	1	2

divs_from_divg_dm_p <- divs_from_divg_dm %>%
    ungroup() %>%
    wilcox_test(divs_after_divergence ~ comparison, paired = T) %>%
    mutate(p=format(p, scientific=T)) %>% 
    add_xy_position(x = "comparison") %>%
    mutate(y.position = y.position+50, p=paste0("p=", p))

divs_from_divg_dm %>% 
    ggplot(aes(comparison, divs_after_divergence)) +
    geom_violin(aes(fill=comparison), 
                 size=2, color="grey23")+
    scale_fill_manual(
        values = c(
            "adenoma_adenoma" = "purple2", "L" = "darkgreen",
            "M" = "orange2", "N" = "grey23", "P" = "firebrick2"
        ),
        guide = "none"
    ) +
   geom_point(color = "grey23", alpha = 0.6, size = 6) +
   geom_line(aes(group = subject), color = "grey23", size = 1, alpha = 0.6) +
   stat_pvalue_manual(divs_from_divg_dm_p, label = "p", tip.length = 0.005, step.increase = 0.01, size = 15, bracket.size = 1) +
   scale_x_discrete(labels = c("Primary\ntumor", "Distant\nmetastases")) +
   labs(y = "Divisions from metastasis divergence to sample") +
   theme_martin() +
   theme(axis.title.x = element_blank())
ggsave("../plots/Figure3/Fig3H.pdf", height = 11, width = 11)

Sample numbers

divs_from_divg_dm %>%
    group_by(comparison) %>%
    count()

A grouped_df: 2 x 2

comparison	n
<fct>	<int>
P	19
M	19

divs_from_divg_ln <- annotated_cmb_cell_divs %>%
    filter((str_detect(a, "N") & !str_detect(b, "N")) | (str_detect(b, "N") & !str_detect(a, "N"))) %>%
    mutate(comparison = ifelse(type_a == "N", type_b, type_a), sample_a = ifelse(str_detect(sample_a, "N"), sample_b, sample_a)) %>%
    left_join(met_sampled_div) %>%
    group_by(subject, comparison) %>%
    left_join(mrca_join_divg) %>%
    mutate(
        across(c(divs, divs_to_divergence), ~ .x - divs_to_mrca), divs_after_divergence = divs-divs_to_divergence,
        fraction_to_divg = divs_to_divergence/divs
    ) %>% 
    mutate(divs = median(divs), divs_to_divergence = median(divs_to_divergence)) %>%
        filter(comparison %in% c("L", "P")) %>%
        group_by(subject) %>%
        fill(divs_to_divergence, .direction = "updown") %>%
        mutate(divs_after_divergence = divs - divs_to_divergence) %>%
        select(subject, divs_after_divergence, comparison) %>%
        distinct() %>%
        add_count() %>%
        filter(n == 2) %>%
        mutate(comparison=fct_relevel(comparison,"P", "L"))

Joining with `by = join_by(subject, sample_a)`
Joining with `by = join_by(subject)`

divs_from_divg_ln_p <- divs_from_divg_ln %>%
    ungroup() %>%
    wilcox_test(divs_after_divergence ~ comparison, paired = T) %>%
    add_significance() %>%
    add_xy_position(x = "comparison") %>%
    mutate(y.position = y.position + 50, p = paste0("p=", p))
divs_from_divg_ln_p

A rstatix_test: 1 x 12

.y.	group1	group2	n1	n2	statistic	p	p.signif	y.position	groups	xmin	xmax
<chr>	<chr>	<chr>	<int>	<int>	<dbl>	<chr>	<chr>	<dbl>	<named list>	<dbl>	<dbl>
divs_after_divergence	P	L	31	31	271	p=0.664	ns	1543.734	P, L	1	2

divs_from_divg_ln %>%
    ggplot(aes(comparison, divs_after_divergence)) +
    geom_violin(aes(fill=comparison), 
                 size=2, color="grey23")+
    scale_fill_manual(
        values = c(
            "adenoma_adenoma" = "purple2", "L" = "darkgreen",
            "M" = "orange2", "N" = "grey23", "P" = "firebrick2"
        ),
        guide = "none"
    ) +
   geom_point(color = "grey23", alpha = 0.6, size = 6) +
   geom_line(aes(group = subject), color = "grey23", size = 1, alpha = 0.6) +
   stat_pvalue_manual(divs_from_divg_ln_p, label = "p", tip.length = 0.005, step.increase = 0.01, size = 15, bracket.size = 1) +
   scale_x_discrete(labels = c("Primary\ntumor", "Lymph node\nmetastasis")) +
   labs(y = "Divisions from metastasis divergence to sample") +
   theme_martin() +
   theme(axis.title.x = element_blank())

ggsave("../plots/Figure3/Extended_Data_Fig6d.pdf", height = 11, width = 6)

Warning message:
"Removed 2 rows containing non-finite outside the scale range
(`stat_ydensity()`)."
Warning message:
"Removed 2 rows containing missing values or values outside the scale range
(`geom_point()`)."
Warning message:
"Removed 2 rows containing missing values or values outside the scale range
(`geom_line()`)."
Warning message:
"Removed 2 rows containing non-finite outside the scale range
(`stat_ydensity()`)."
Warning message:
"Removed 2 rows containing missing values or values outside the scale range
(`geom_point()`)."
Warning message:
"Removed 2 rows containing missing values or values outside the scale range
(`geom_line()`)."

Sample numbers

divs_from_divg_ln %>%
    ungroup() %>% 
    count(comparison)

A tibble: 2 x 2

comparison	n
<fct>	<int>
P	32
L	32

Fig 3I

divg_time_plot_data <- patient_mrca %>%
    select(-comparison) %>%
    left_join(divergence_timing) %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>% 
    filter(comparison != "adenoma_adenoma",!((subject %in% meta_subjects) & comparison=="met_primary")) %>%
    mutate(mrca = mrca - divs) %>%
    group_by(comparison, subject) %>%
    summarize(mrca = median(mrca)) %>%
    ungroup() %>%
    mutate(comparison = fct_relevel(
        comparison,
        "primary_primary", "ln_primary", "met_primary"
    ))

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'comparison'. You can override using the
`.groups` argument.

p_pt_ln <- divg_time_plot_data %>%
    group_by(subject) %>%
    filter(comparison == "primary_primary" | comparison == "ln_primary") %>%
    add_count() %>%
    filter(n > 1) %>%
    ungroup() %>%
    mutate(comparison = as.character(comparison)) %>%
    wilcox_test(mrca ~ comparison, paired = T) 

p_pt_met <- divg_time_plot_data %>%
    group_by(subject) %>%
    filter(comparison == "primary_primary" | comparison == "met_primary") %>%
    add_count() %>%
    filter(n > 1) %>%
    ungroup() %>%
    mutate(comparison = as.character(comparison)) %>%
    wilcox_test(mrca ~ comparison, paired = T)

bind_rows(p_pt_ln, p_pt_met) %>%
    adjust_pvalue() %>%
    mutate(p=format(p, scientific=T))

A rstatix_test: 2 x 8

.y.	group1	group2	n1	n2	statistic	p	p.adj
<chr>	<chr>	<chr>	<int>	<int>	<dbl>	<chr>	<dbl>
mrca	ln_primary	primary_primary	31	31	319	1.69e-01	0.169000
mrca	met_primary	primary_primary	19	19	180	1.64e-04	0.000328

divg_time_plot_data %>%
    count(comparison)

A tibble: 3 x 2

comparison	n
<fct>	<int>
primary_primary	36
ln_primary	31
met_primary	19

divg_time_plot_data %>% 
    ggplot(aes(comparison, mrca)) +
    geom_quasirandom(aes(fill = comparison), width = 0.3, size = 9, pch = 21, color = "grey23", stroke = 1, show.legend = FALSE) +
    geom_boxplot(alpha = 0, size = 1.5, color = "grey23") +
    scale_fill_manual(values = c(
        "primary_primary"="firebrick2",
        "ln_primary"="darkgreen",
        "met_primary"="orange2"),
                       guide="none") +
    scale_x_discrete(labels= c(
        "Primary tumor\ndiversification",
        "Lymph node\nmetastasis\ndivergence",
        "Distant\nmetastasis\ndivergence"
        )) +
    geom_point(aes(x = "met_primary", y = 3300), alpha = 0) +
    scale_y_break(c(1250, 2000), ticklabels = 2500, scales = 0.18, space = 0.01) +
    ylim(-100, 4000) +
    theme_martin() +
    theme(
        text = element_text(size = 20, color = "black"),
        axis.text = element_text(color = "black"),
        axis.ticks = element_line(color = "black"), axis.text.y.right = element_blank(), axis.ticks.y.right = element_blank(),
        axis.line.y.right = element_blank(), axis.title.y.left = element_blank(), axis.title.x = element_blank()
    ) 
ggsave("../plots/Figure3/Fig3I.pdf", height = 11, width = 11)

Comparing metachronous metastases separately

timing_p_ln <- patient_mrca %>%
    select(-comparison) %>%
    left_join(divergence_timing) %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    filter(comparison != "adenoma_adenoma") %>%
    mutate(mrca = mrca - divs) %>%
    group_by(comparison, subject) %>%
    summarize(mrca = median(mrca)) %>%
    ungroup() %>%
    filter(comparison != "met_primary") %>%
    group_by(subject) %>%
    add_count() %>%
    filter(n > 1) %>%
    ungroup() %>%
    wilcox_test(mrca ~ comparison, paired = T) 

timing_p_met <- patient_mrca %>%
    select(-comparison) %>%
    left_join(divergence_timing) %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    filter(comparison != "adenoma_adenoma") %>%
    mutate(mrca = mrca - divs) %>%
    group_by(comparison, subject) %>%
    summarize(mrca = median(mrca)) %>%
    ungroup() %>%
    filter(comparison != "ln_primary") %>%
    group_by(subject) %>%
    add_count() %>%
    filter(n > 1) %>%
    ungroup() %>%
    wilcox_test(mrca ~ comparison, paired = T)
    

bind_rows(timing_p_ln, timing_p_met) %>%
    adjust_pvalue() %>%
    mutate(p.adj=format(p.adj, scientific=T))

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'comparison'. You can override using the
`.groups` argument.
Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'comparison'. You can override using the
`.groups` argument.

A rstatix_test: 2 x 8

.y.	group1	group2	n1	n2	statistic	p	p.adj
<chr>	<chr>	<chr>	<int>	<int>	<dbl>	<dbl>	<chr>
mrca	ln_primary	primary_primary	31	31	319	0.169000	1.69e-01
mrca	met_primary	primary_primary	26	26	312	0.000217	4.34e-04

patient_mrca %>%
    select(-comparison) %>%
    left_join(divergence_timing) %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    filter(comparison != "adenoma_adenoma") %>%
    mutate(mrca = mrca - divs) %>%
    group_by(comparison, subject) %>%
    summarize(mrca = median(mrca)) %>%
    ungroup() %>%
    mutate(comparison = fct_relevel(
        comparison,
        "primary_primary", "ln_primary", "met_primary"
    )) %>%
    ggplot(aes(comparison, mrca)) +
    geom_quasirandom(aes(fill = comparison), width = 0.3, size = 9, pch = 21, color = "grey23", stroke = 1) +
    geom_boxplot(alpha = 0, size = 1, color = "grey23") +
    scale_fill_manual(values = c("A"="purple2", "ln_primary"="darkgreen", 
                                  "met_primary"="orange2", "M_meta"="orange3","N"="grey23", "primary_primary"="firebrick2"),
                       guide="none") +
    scale_x_discrete(labels= c(
        "Primary tumor\ndiversification",
        "Lymph node\nmetastasis\ndivergence",
        "Distant\nmetastasis\ndivergence\n(including metachronous)"
        )) + 
    scale_y_break(c(1250, 2000), ticklabels = 2500, scales = 0.18, space = 0.01) +
    ylim(-100, 4000) +
    theme_martin() +
    theme(
        text = element_text(size = 20, color = "black"),
        axis.text = element_text(color = "black"),
        axis.ticks = element_line(color = "black"), axis.text.y.right = element_blank(), axis.ticks.y.right = element_blank(),
        axis.line.y.right = element_blank(), axis.title.y.left = element_blank(), axis.title.x = element_blank()
    ) +
        labs(y="Divisions from MRCA") 
ggsave("../plots/Figure3/Extended_Data_Fig6f.pdf", height = 11, width = 14)

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'comparison'. You can override using the
`.groups` argument.

patient_mrca %>%
    select(-comparison) %>%
    left_join(divergence_timing) %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    filter(comparison != "adenoma_adenoma") %>%
    mutate(mrca = mrca - divs) %>%
    group_by(comparison, subject) %>%
    summarize(mrca = median(mrca)) %>%
    ungroup() %>%
    mutate(comparison = fct_relevel(
        comparison,
        "primary_primary", "ln_primary", "met_primary"
    )) %>% 
    count(comparison)

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'comparison'. You can override using the
`.groups` argument.

A tibble: 3 x 2

comparison	n
<fct>	<int>
primary_primary	36
ln_primary	31
met_primary	26

Extended Data Fig 4

Bootstrapping key steps of cancer evolution on the patient level.

# generated in sample processing step
l <- readRDS("../results/bootstrapped_crc_trees.rds")

Cancer MRCA of all cases

extract_mrca_fast <- function(tree){
  
  # finding the mrca of all tumor samples
  tumors <-  c(str_subset(tree$tip.label, "N|Ad", negate = TRUE))
  findMRCA(tree, tumors, type = "height")
 
}

mrca_numbers <- l %>%
    list_flatten() %>%
    purrr::map(extract_mrca_fast)

subjects_bs <- unique(markerlengths$subject)

mrca_bootstraps <- tibble(x = unlist(mrca_numbers))
subject_mrca_bootstraps <- tibble(x = unlist(mrca_numbers), subject=rep(subjects_bs, each=1000))

observed_mrcas <- mrca_tbl %>%
    select(1:2)
cohort_mrca_median <- median(observed_mrcas$all_mrca)

subject_mrca_bootstraps %>%
    group_by(subject) %>%
    summarize(median = median(x), twofive = quantile(x, 0.025), ninesevenfive = quantile(x, 0.975)) %>%
    left_join(observed_mrcas) %>% 
    ggplot(aes(all_mrca, reorder(subject, median))) +
    geom_segment(aes(x = twofive, xend = ninesevenfive, y = reorder(subject, all_mrca), yend = reorder(subject, all_mrca)), lineend = "round", size = 9, alpha = 0.3, color = "grey42") +
    geom_point(size = 9, color = "grey42") +
    geom_vline(xintercept = cohort_mrca_median, linetype = 2, color = "grey42", size = 1) +
    labs(y = "Subject", x = "Divisions from zygote to cancer MRCA") +
    theme_martin()
ggsave("../plots/Figure3/Extended_Data_Fig5a.pdf", height = 20, width = 17)

Joining with `by = join_by(subject)`

Primary tumor diversification

timing_pt_divergence <- function(tree) {
  
  # find unique lesions 
  unique_lesions <- tree$tip.label %>% 
    str_remove("[:alpha:]$") %>% 
    str_subset("M|L") %>% 
    unique()

  # finding the mrca of all tumor samples
  tumors <-  c(str_subset(tree$tip.label, "N|Ad", negate = TRUE))
  all_mrca <-  findMRCA(tree, tumors, type = "height")
  
  met_primary_mrca <- lapply(unique_lesions, get_lesion_primary_mrca_dist, tree)
  
  # all primary tumor samples
  p_samples <- tree$tip.label %>%
    str_subset("P")
  
 primary_primary_mrca <- NULL 
 if (length(p_samples) > 1) {
   # all unique combinations of primary tumor samples
   cbm <- combn(p_samples, m = 2) %>% as.data.frame()

   primary_primary_mrca <- lapply(1:ncol(cbm), get_primary_primary_mrca_dist, cbm, tree)
  }

  return(bind_rows(primary_primary_mrca, met_primary_mrca) %>%
    mutate(mrca = mrca-all_mrca))
 
}

flat <- l %>%
    list_flatten()

landmark_timings <- flat %>%
    parallel::mclapply(timing_pt_divergence)

names(landmark_timings) <- paste0(rep(subjects_bs, each=1000), "_", rep(1:1000, 37))

landmarkts_tbl <- list_rbind(landmark_timings, names_to = "subject")

landmarkts_tbl %>%
    write_tsv("../results/bootstrapped_landmark_tbl.tsv")

landmarkts_tbl <- read_tsv("../results/bootstrapped_landmark_tbl.tsv")

Rows: 644000 Columns: 4
-- Column specification --------------------------------------------------------
Delimiter: "\t"
chr (3): subject, samples, comparison
dbl (1): mrca

i Use `spec()` to retrieve the full column specification for this data.
i Specify the column types or set `show_col_types = FALSE` to quiet this message.

# patient median divergence timing
pat_med_divg <- patient_mrca %>%
    select(-comparison) %>%
    left_join(divergence_timing) %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    filter(comparison != "adenoma_adenoma") %>%
    mutate(mrca = mrca - divs) %>%
    group_by(comparison, subject) %>%
    summarize(mrca = median(mrca))

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'comparison'. You can override using the
`.groups` argument.

summary_tbl <- landmarkts_tbl %>%
    # C63 only has one sample of the primary tumor, so there is no ground truth in terms of divergence timing
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>% 
    separate(subject, c("subject", "rep")) %>%
    filter(subject != "C63") %>% 
    group_by(subject, rep, comparison) %>%
    summarize(divs = median(mrca)) %>%
    group_by(subject, comparison) %>%
    summarize(median = median(divs), twofive = quantile(divs, 0.025), ninesevenfive = quantile(divs, 0.975))

`summarise()` has grouped output by 'subject', 'rep'. You can override using
the `.groups` argument.
`summarise()` has grouped output by 'subject'. You can override using the
`.groups` argument.

Primary tumor diversification

pt_divs_tbl <- pat_med_divg %>%
    filter(comparison == "primary_primary") %>%
    rename(pt_divs=mrca)
pt_divs_median <- median(pt_divs_tbl$pt_divs)

summary_tbl %>%
    filter(comparison == "primary_primary") %>%
    left_join(pt_divs_tbl) %>% 
    ggplot(aes(pt_divs, reorder(subject, pt_divs))) +
    geom_segment(aes(x = twofive, xend = ninesevenfive, y = reorder(subject, pt_divs), yend = reorder(subject, pt_divs)), lineend = "round", size = 9, alpha = 0.3, color = "firebrick2") +
    geom_point(size = 9, color = "firebrick2") +
    geom_vline(xintercept = pt_divs_median, linetype = 2, color = "firebrick2", size = 1) +
    labs(y = "Subject", x = "Divisions from MRCA to primary tumor diversification") +
    theme_martin()
ggsave("../plots/Figure3/Extended_Data_Fig5b.pdf", height = 20, width = 17)

Joining with `by = join_by(subject, comparison)`

Distant metastasis divergence

met_divs_tbl <- pat_med_divg %>%
    filter(comparison == "met_primary") %>%
    rename(met_divs=mrca)
met_divs_median <- median(met_divs_tbl$met_divs)

summary_tbl %>%
    filter(comparison == "met_primary") %>%
    left_join(met_divs_tbl) %>% 
    ggplot(aes(met_divs, reorder(subject, met_divs))) +
    geom_segment(aes(x = twofive, xend = ninesevenfive, y = reorder(subject, met_divs), yend = reorder(subject, met_divs)), lineend = "round", size = 9, alpha = 0.3, color = "orange2") +
    geom_point(size = 9, color = "orange2") +
    geom_vline(xintercept = met_divs_median, linetype=2, color = "orange3", size=1) +
    labs(y="Subject", x="Divisions from MRCA to distant metastasis divergence") +
    theme_martin()
ggsave("../plots/Figure3/Extended_Data_Fig5d.pdf", height = 20, width = 17)

Joining with `by = join_by(subject, comparison)`

Lymph node metastasis divergence

ln_divs_tbl <- pat_med_divg %>%
    filter(comparison == "ln_primary") %>%
    rename(ln_divs = mrca)
ln_divs_median <- median(ln_divs_tbl$ln_divs)

summary_tbl %>%
    filter(comparison == "ln_primary") %>%
    left_join(ln_divs_tbl) %>% 
    ggplot(aes(ln_divs, reorder(subject, ln_divs))) +
    geom_segment(aes(x = twofive, xend = ninesevenfive, y = reorder(subject, ln_divs), yend = reorder(subject, ln_divs)), lineend = "round", size = 9, alpha = 0.3, color = "darkgreen") +
    geom_point(size = 9, color = "darkgreen") +
    geom_vline(xintercept = ln_divs_median, linetype = 2, color = "darkgreen", size = 1) +
    labs(y = "Subject", x = "Divisions from MRCA to lymph node metastasis divergence") +
    theme_martin()
ggsave("../plots/Figure3/Extended_Data_Fig5c.pdf", height = 20, width = 17)

Joining with `by = join_by(subject, comparison)`

Fig 3J

Divisions of primary tumor sample clostest to mets

# excluding early seeding events
early_seeding <- divergence_timing %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    group_by(subject, comparison) %>%
    summarize(mrca = median(mrca)) %>%
    mutate(mrca = mrca - mrca[comparison == "primary_primary"]) %>%
    filter(comparison == "met_primary", mrca < 0) %>%
    pull(subject)

# finding the primary tumor samples that have the smallest distance to any met sample
min_met_dist_sample <- long_mrca_tbl %>%
    filter(comparison == "all_mrca") %>%
    left_join(annotated_cmb_cell_divs) %>%
    filter((str_detect(a, "P") & str_detect(b, "M")) | (str_detect(b, "P") & str_detect(a, "M"))) %>%
    mutate(met_lesion = ifelse(str_detect(sample_a, "M"), sample_a, sample_b)) %>% 
    group_by(subject, met_lesion) %>% 
    slice_min(divs) %>% 
    mutate(min_met_dist_sample = ifelse(str_detect(a, "P"), a, b)) %>% 
    pull(min_met_dist_sample)

`summarise()` has grouped output by 'subject'. You can override using the
`.groups` argument.
Joining with `by = join_by(subject)`

seeding_region_tbl <- long_mrca_tbl %>%
    filter(comparison == "all_mrca") %>%
    left_join(annotated_cmb_cell_divs) %>%
    group_by(subject) %>%
    filter((str_detect(a, "N") | str_detect(b, "N"))) %>%
    filter(str_detect(a, "P") | str_detect(b, "P")) %>%
    mutate(divs_from_mrca = divs - mrca_divs, met_adjacent = ifelse(a %in% min_met_dist_sample | b %in% min_met_dist_sample, TRUE, FALSE)) %>%
    group_by(subject, met_adjacent) %>%
    summarize(divs_from_mrca = median(divs_from_mrca)) %>%
    group_by(subject) %>%
    filter(n() == 2) %>%
    ungroup() %>%
    filter(!(subject %in% early_seeding))

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'subject'. You can override using the
`.groups` argument.

paired_p <- seeding_region_tbl %>%
    wilcox_test(divs_from_mrca ~ met_adjacent, paired = T) %>%
    add_xy_position(x = "met_adjacent") %>%
    mutate(y.position = 3500)  %>% 
    p_format(trailing.zero = TRUE, digits = 3, accuracy = 1e-03, add.p = TRUE) %>% 
    mutate(p=str_pad(p, 7, "0", side="right"))
paired_p

A rstatix_test: 1 x 11

.y.	group1	group2	n1	n2	statistic	p	y.position	groups	xmin	xmax
<chr>	<chr>	<chr>	<int>	<int>	<dbl>	<chr>	<dbl>	<named list>	<dbl>	<dbl>
divs_from_mrca	FALSE	TRUE	24	24	79	p=0.0425	3500	FALSE, TRUE	1	2

seeding_medians <- seeding_region_tbl %>%
    group_by(met_adjacent) %>%
    summarise(divs_from_mrca = median(divs_from_mrca)) %>% 
    mutate(met_adjacent = ifelse(met_adjacent, "adjacent", "not_adjacent"), met_adjacent = fct_relevel(met_adjacent, "not_adjacent", "adjacent"))

seeding_region_tbl %>%
    group_by(subject) %>%
    filter(divs_from_mrca[met_adjacent] > divs_from_mrca[!met_adjacent]) %>%
    pull(subject) %>%
    unique()

1. 'C100'
2. 'C12'
3. 'C31'
4. 'C36'
5. 'C38'
6. 'C45'
7. 'C46'
8. 'C51'
9. 'C57'
10. 'C59'
11. 'C66'
12. 'C70'
13. 'C77'
14. 'C80'
15. 'C89'
16. 'C90'
17. 'C97'
18. 'C99'

seeding_region_tbl %>%
    mutate(met_adjacent = ifelse(met_adjacent, "adjacent", "not_adjacent"), met_adjacent = fct_relevel(met_adjacent, "not_adjacent", "adjacent")) %>%
    ggplot(aes(met_adjacent, divs_from_mrca)) +
    geom_line(aes(group = subject), color = "grey23", size = 1, alpha = 0.6) +
    geom_point(aes(fill = met_adjacent), size = 9, pch = 21, color = "grey23", stroke = 1, show.legend = FALSE) +
    geom_point(data=seeding_medians, color="grey23", shape="-", size=30) +
    scale_y_break(c(1500, 2800), ticklabels = 3000, scales = 0.18, space = 0.01) +
    ylim(0, 3500) +
    scale_fill_manual(
        values = c(
            "adjacent" = "darkorange2", "not_adjacent" = "firebrick2"
        ),
        guide = "none"
    ) +
    scale_x_discrete(labels = c("Other primary\ntumor regions", "Clostest region\nto metastasis")) +
        labs(y = "Divisions from MRCA") +
        theme_martin() +
        theme(axis.title.x = element_blank(), axis.title.y = element_blank(),  axis.title.y.right  = element_blank(),
            axis.text.y.right  = element_blank(), axis.ticks.y.right  = element_blank(), axis.line.y.right  = element_blank())
ggsave("../plots/Figure3/Fig3J.pdf", height = 11, width = 11)

Same analysis for lymph node metastases:

# excluding early seeding events
early_seeding_ln <- divergence_timing %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    group_by(subject, comparison) %>%
    summarize(mrca = median(mrca)) %>%
    mutate(mrca = mrca - mrca[comparison == "primary_primary"]) %>%
    filter(comparison == "ln_primary", mrca < 0) %>%
    pull(subject)

# finding the primary tumor samples that have the smallest distance to any met sample
min_met_dist_sample_ln <- long_mrca_tbl %>%
    filter(comparison == "all_mrca") %>%
    left_join(annotated_cmb_cell_divs) %>%
    filter((str_detect(a, "P") & str_detect(b, "L")) | (str_detect(b, "P") & str_detect(a, "L"))) %>%
    mutate(met_lesion = ifelse(str_detect(sample_a, "L"), sample_a, sample_b)) %>% 
    group_by(subject, met_lesion) %>% 
    slice_min(divs) %>% 
    mutate(min_met_dist_sample = ifelse(str_detect(a, "P"), a, b)) %>% 
    pull(min_met_dist_sample)

`summarise()` has grouped output by 'subject'. You can override using the
`.groups` argument.
Joining with `by = join_by(subject)`

seeding_region_tbl_ln <- long_mrca_tbl %>%
    filter(comparison == "all_mrca") %>%
    left_join(annotated_cmb_cell_divs) %>%
    group_by(subject) %>%
    filter((str_detect(a, "N") | str_detect(b, "N"))) %>%
    filter(str_detect(a, "P") | str_detect(b, "P")) %>%
    mutate(divs_from_mrca = divs - mrca_divs, met_adjacent = ifelse(a %in% min_met_dist_sample_ln | b %in% min_met_dist_sample_ln, TRUE, FALSE)) %>%
    group_by(subject, met_adjacent) %>%
    summarize(divs_from_mrca = median(divs_from_mrca)) %>%
    group_by(subject) %>%
    filter(n() == 2) %>%
    ungroup() %>%
    filter(!(subject %in% early_seeding_ln))

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'subject'. You can override using the
`.groups` argument.

paired_p <- seeding_region_tbl_ln %>%
    wilcox_test(divs_from_mrca ~ met_adjacent, paired = T) %>%
    add_xy_position(x = "met_adjacent") %>%
    mutate(y.position = 3500)  %>% 
    p_format(trailing.zero = TRUE, digits = 3, accuracy = 1e-03, add.p = TRUE) %>% 
    mutate(p=str_pad(p, 7, "0", side="right"))
paired_p

A rstatix_test: 1 x 11

.y.	group1	group2	n1	n2	statistic	p	y.position	groups	xmin	xmax
<chr>	<chr>	<chr>	<int>	<int>	<dbl>	<chr>	<dbl>	<named list>	<dbl>	<dbl>
divs_from_mrca	FALSE	TRUE	18	18	104	p=0.442	3500	FALSE, TRUE	1	2

seeding_medians_ln <- seeding_region_tbl_ln %>%
    group_by(met_adjacent) %>%
    summarise(divs_from_mrca = median(divs_from_mrca)) %>% 
    mutate(met_adjacent = ifelse(met_adjacent, "adjacent", "not_adjacent"), met_adjacent = fct_relevel(met_adjacent, "not_adjacent", "adjacent"))

seeding_region_tbl_ln %>%
    mutate(met_adjacent = ifelse(met_adjacent, "adjacent", "not_adjacent"), met_adjacent = fct_relevel(met_adjacent, "not_adjacent", "adjacent")) %>%
    ggplot(aes(met_adjacent, divs_from_mrca)) +
    geom_line(aes(group = subject), color = "grey23", size = 1, alpha = 0.6) +
    geom_point(aes(fill = met_adjacent), size = 9, pch = 21, color = "grey23", stroke = 1, show.legend = FALSE) +
    geom_point(data=seeding_medians_ln, color="grey23", shape="-", size=30) +
    scale_y_break(c(1500, 2800), ticklabels = 3000, scales = 0.18, space = 0.01) +
    ylim(0, 3500) +
    #stat_pvalue_manual(paired_p, label = "p", tip.length = 0.005, step.increase = 0.01, size = 15, bracket.size = 1) +
    scale_fill_manual(
        values = c(
            "adjacent" = "darkgreen", "not_adjacent" = "firebrick2"
        ),
        guide = "none"
    ) +
    scale_x_discrete(labels = c("Other primary\ntumor regions", "Clostest region\nto lymph node\nmetastasis")) +
        labs(y = "Divisions from MRCA") +
        theme_martin() +
        theme(axis.title.x = element_blank(), axis.title.y = element_blank(),  axis.title.y.right  = element_blank(),
            axis.text.y.right  = element_blank(), axis.ticks.y.right  = element_blank(), axis.line.y.right  = element_blank())
ggsave("../plots/Figure3/Extended_Data_Fig6h.pdf", height = 11, width = 11)

Timing when metastases could have diverged

divergence_timing %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    filter(str_detect(comparison, "met")) %>%
    left_join(patient_mrca, by=c("subject")) %>%
    mutate(
        mrca_diff = mrca - divs,
        years_from_mrca = mrca_diff / 91.25
    ) %>%
    group_by(subject) %>%
    summarize(min = min(years_from_mrca), max = max(years_from_mrca), years_from_mrca = median(years_from_mrca), n=n()) %>%
    ggplot(aes(reorder(subject, years_from_mrca), years_from_mrca)) +
    geom_hline(yintercept = 16, color="white", size=20) +
    geom_hline(yintercept = 24, color="white", size=20) +
    geom_pointrange(aes(ymin = min, ymax = max, group = subject, color = log2(years_from_mrca + 1)), size = 4.3,
    linewidth=4.3,
    show.legend = FALSE) +
    geom_text(aes(label=n), color="white", size=12, fontface = "bold") +
    scale_colour_gradient(low = "orange2", high = "firebrick2") +
    scale_y_break(c(15, 25),  ticklabels=c(30), scales=0.15) +
    scale_y_reverse(
       "Years after tumor initation (4d / division)",
       limits=c(35,0)
     ) +
    scale_x_discrete(expand = expansion(mult = 0, add = 1)) +
        theme_martin() +
        theme(
            axis.title.x = element_blank(), axis.text.x = element_text(angle = 45, hjust = 1),
            panel.grid.major.x = element_line(size = 1.5, color = "grey85", linetype = 3), axis.title.y.right = element_blank(),
            axis.text.y.right = element_blank(), axis.ticks.y.right = element_blank(), axis.line.y.right = element_blank()
        )
    ggsave("../plots/Figure3/Extended_Data_Fig6i.pdf", height = 11, width = 24)

Years from cancer MRCA to metastasis divergence

tumor_mrca <- long_mrca_tbl %>%
    filter(comparison=="all_mrca") %>% 
    select(subject, mrca_divs)

divergence_timing %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    filter(str_detect(comparison, "met")) %>%
    left_join(tumor_mrca) %>%
    mutate(
        mrca_diff = mrca - mrca_divs,
        years_from_mrca = mrca_diff / 91.25
    ) %>%
    group_by(subject) %>%
    summarize(min = min(years_from_mrca), max = max(years_from_mrca), years_from_mrca = median(years_from_mrca)) %>% 
    summarize(min(years_from_mrca), max(years_from_mrca), median(years_from_mrca))

Joining with `by = join_by(subject)`

A tibble: 1 x 3

min(years_from_mrca)	max(years_from_mrca)	median(years_from_mrca)
<dbl>	<dbl>	<dbl>
0	30.5586	5.559582

# finding number of division from tumor MRCA to median of primary samples
# works as a surrogate for cell divisions at diagnosis
diag_divs <- tumor_ad_mrca %>%
    left_join(annotated_cmb_cell_divs) %>%
    group_by(subject) %>%
    filter((str_detect(a, "N") & str_detect(b, "P")) | str_detect(a, "P") & str_detect(b, "N")) %>%
    mutate(divs_from_mrca=divs-mrca_divs) %>% 
    summarize(pt_divs_from_mrca=median(divs_from_mrca))

Joining with `by = join_by(subject)`

divergence_timing %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    filter(str_detect(comparison, "met")) %>%
    left_join(tumor_mrca) %>%
    mutate(
        mrca_diff = mrca - mrca_divs,
        years_from_mrca = mrca_diff / 91.25
    ) %>%
    group_by(subject) %>%
        summarize(min = min(years_from_mrca), max = max(years_from_mrca), years_from_mrca = median(years_from_mrca), mrca_diff = median(mrca_diff)) %>%
        left_join(diag_divs) %>%
        mutate(divs_before_diag = pt_divs_from_mrca - mrca_diff, years_before_diag = divs_before_diag / 91.25) %>%
        summarize(min(years_before_diag),max(years_before_diag),median(years_before_diag))

Joining with `by = join_by(subject)`
Joining with `by = join_by(subject)`

A tibble: 1 x 3

min(years_before_diag)	max(years_before_diag)	median(years_before_diag)
<dbl>	<dbl>	<dbl>
-4.94797	12.74962	2.304485

Fig 3K

# mrca of all samples
median_mrca_tbl <- long_mrca_tbl %>%
    filter(comparison == "all_mrca") %>%
    filter(!(subject %in% msi_tumors)) %>%
    select(-sample_type) %>%
    rename(divs = mrca_divs) %>%
    group_by(comparison) %>%
    summarize(divs=median(divs))

median_mrca <- median_mrca_tbl$divs

# primary and adenoma diversification + met and ln divergence
divg_med_tbl <- patient_mrca %>%
    select(-comparison) %>%
    left_join(divergence_timing) %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    mutate(mrca = mrca - divs) %>%
    group_by(comparison, subject) %>%
    summarise(divs = median(mrca)) %>% 
    summarise(divs = median(divs)) %>% 
    filter(comparison!="adenoma_adenoma") %>% 
    drop_na()

# divs from zygote to sample type
divs_to_sample_med_tbl <- plot_divs_from_mrca %>%
    rename(comparison=sample_type) %>% 
    group_by(comparison) %>%
    summarise(divs = median(divs_from_mrca))

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'comparison'. You can override using the
`.groups` argument.

bind_rows(median_mrca_tbl, divg_med_tbl, divs_to_sample_med_tbl) %>%
    mutate(divs = ifelse(comparison != "all_mrca", divs + divs[comparison == "all_mrca"], divs)) %>%
    drop_na() %>% 
    mutate(comparison = fct_reorder(comparison, divs)) %>%
    ggplot(aes(comparison, divs, color = comparison)) +
    geom_segment(aes(x = comparison, xend = comparison, y = 0, yend = divs), size = 3, lineend = "round") +
    geom_segment(aes(x = -5, xend = comparison, y = divs, yend = divs), size = 3, lineend = "round", linetype = 2) +
    scale_color_manual(
        values = c(
            "L" = "darkgreen", "ln_primary" = "darkgreen",
            "M" = "orange2", "met_primary" = "orange2", "all_mrca" = "grey42",
            "P" = "firebrick2", "primary_primary" = "firebrick2"
        ),
        guide = "none"
    ) +
    scale_y_continuous(breaks=seq(0,3000, 500)) +
    coord_cartesian(ylim = c(2800, 0), xlim=c(-1,7.5)) +
    labs(y = "Cell divisions") +
    theme_martin() +
    theme(
        axis.line.x = element_blank(), axis.title.x = element_blank(),
        axis.text.x = element_blank(),
        axis.ticks.x = element_blank()
    )
ggsave("../plots/Figure3/Fig3K.pdf", height = 20, width = 16)

Estimating effective division rate

plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(
        volume = pi / 6 * size * (size / 2)^2, cell_count = volume * 10e8, growth_rate = cell_count^(1 / pt_divs),
        death_rate=1-(growth_rate-1), death_birth_ratio=death_rate/1
    ) %>% 
    summarize(median(growth_rate), median(death_birth_ratio), n=n())

Joining with `by = join_by(subject)`

A tibble: 1 x 3

median(growth_rate)	median(death_birth_ratio)	n
<dbl>	<dbl>	<int>
1.028744	0.9712565	37

plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(
        volume = pi / 6 * size * (size / 2)^2, cell_count = volume * 10e8, growth_rate = cell_count^(1 / pt_divs),
        death_rate=1-(growth_rate-1), death_birth_ratio=death_rate/1
    ) %>% 
    mutate(MSS_status = ifelse(subject %in% msi_tumors, "MSI", "MSS"), MSS_status = fct_relevel(MSS_status, "MSS", "MSI")) %>%
    group_by(MSS_status) %>% 
    summarize(median(death_birth_ratio), n=n())

Joining with `by = join_by(subject)`

A tibble: 2 x 3

MSS_status	median(death_birth_ratio)	n
<fct>	<dbl>	<int>
MSS	0.9712565	31
MSI	0.9717346	6

plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(
        volume = pi / 6 * size * (size / 2)^2, cell_count = volume * 10e8, death_birth_ratio=((pt_divs/2)-log(cell_count))/(pt_divs/2)
    ) %>% 
    summarize(median(death_birth_ratio), format(median(cell_count), scientific=T), median(pt_divs), n = n())

Joining with `by = join_by(subject)`

A tibble: 1 x 4

median(death_birth_ratio)	format(median(cell_count), scientific = T)	median(pt_divs)	n
<dbl>	<chr>	<dbl>	<int>
0.9433236	1.192823e+10	799.7295	37

plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(
        volume = pi / 6 * size * (size / 2)^2, cell_count = volume * 10e8, death_birth_ratio=((pt_divs/2)-log(cell_count))/(pt_divs/2)
    ) %>% 
    mutate(MSS_status = ifelse(subject %in% msi_tumors, "MSI", "MSS"), MSS_status = fct_relevel(MSS_status, "MSS", "MSI")) %>%
    group_by(MSS_status) %>% 
    summarize(median(death_birth_ratio), format(median(cell_count), scientific=T), median(pt_divs), n = n())

Joining with `by = join_by(subject)`

A tibble: 2 x 5

MSS_status	median(death_birth_ratio)	format(median(cell_count), scientific = T)	median(pt_divs)	n
<fct>	<dbl>	<chr>	<dbl>	<int>
MSS	0.9433236	1.192823e+10	799.7295	31
MSI	0.9442639	7.125374e+10	910.7904	6

plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(
        volume = (pi*size^3)/6, cell_count = volume * 10e8, death_birth_ratio=((pt_divs/2)-log(cell_count))/(pt_divs/2)
    ) %>% 
    mutate(MSS_status = ifelse(subject %in% msi_tumors, "MSI", "MSS"), MSS_status = fct_relevel(MSS_status, "MSS", "MSI")) %>%
    summarize(median(death_birth_ratio), format(median(cell_count), scientific=T), median(pt_divs), n = n())

Joining with `by = join_by(subject)`

A tibble: 1 x 4

median(death_birth_ratio)	format(median(cell_count), scientific = T)	median(pt_divs)	n
<dbl>	<chr>	<dbl>	<int>
0.9400654	4.771294e+10	799.7295	37

plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(
        volume = pi / 6 * size * (size / 2)^2, cell_count = volume * 10e8, death_birth_ratio = ((pt_divs / 2) - log(cell_count)) / (pt_divs / 2)
    ) %>%
    mutate(MSS_status = ifelse(subject %in% msi_tumors, "MSI", "MSS"), MSS_status = fct_relevel(MSS_status, "MSS", "MSI")) %>%
        group_by(MSS_status) %>%
        write_tsv("../results/crc_death_birth_rates.tsv")

Joining with `by = join_by(subject)`

plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(
        volume = (pi*size^3)/6, cell_count = volume * 10e8, death_birth_ratio = ((pt_divs / 2) - log(cell_count)) / (pt_divs / 2)
    ) %>%
    mutate(MSS_status = ifelse(subject %in% msi_tumors, "MSI", "MSS"), MSS_status = fct_relevel(MSS_status, "MSS", "MSI")) %>%
    group_by(MSS_status) %>% 
    summarize(median(death_birth_ratio), n=n())

Joining with `by = join_by(subject)`

A tibble: 2 x 3

MSS_status	median(death_birth_ratio)	n
<fct>	<dbl>	<int>
MSS	0.9400654	31
MSI	0.9411699	6

options(repr.plot.width=7, repr.plot.height=7)
plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(
        volume = pi / 6 * size * (size / 2)^2, cell_count = volume * 10e8, death_birth_ratio = ((pt_divs / 2) - log(cell_count)) / (pt_divs / 2)
    ) %>%
    mutate(MSS_status=ifelse(subject %in% msi_tumors, "MSI", "MSS"), MSS_status=fct_relevel(MSS_status, "MSI", "MSS")) %>% 
    ggplot(aes(MSS_status, death_birth_ratio)) +
    geom_quasirandom(aes(fill = MSS_status), width = 0.3, size = 9, pch = 21, color = "grey23", stroke = 1) +
    geom_boxplot(alpha=0, size=1, color="grey23") +
    scale_fill_brewer(palette = "Set2",
                       guide="none") +
    # stat_pvalue_manual(msi_mss_p, tip.length = 0.03, step.increase = 0.01, size = 10, bracket.size = 1, bracket.nudge.y = 100) +
    scale_x_discrete(labels = c("MMRd", "MMRp")) +
        # coord_cartesian(ylim=c(0,6000)) +
        labs(y = "Death rate to birth rate ratio") +
        theme_martin() +
        theme(axis.title.x = element_blank())
ggsave("../plots/Supplementary_figures/SupNote5Fig1.pdf", height=7, width=7)

Joining with `by = join_by(subject)`

plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(
        volume = (pi*size^3)/6, cell_count = volume * 1e9, growth_rate = cell_count^(1 / pt_divs),
        death_rate=1-(growth_rate-1), death_birth_ratio=death_rate/1, test=2-death_rate
    ) %>% 
    summarize(median(death_rate), median(growth_rate))

Joining with `by = join_by(subject)`

A tibble: 1 x 2

median(death_rate)	median(growth_rate)
<dbl>	<dbl>
0.9695792	1.030421

plot_divs_from_mrca %>%
    filter(sample_type == "P") %>%
    group_by(subject) %>%
    filter(!is.na(divs_from_mrca)) %>%
    summarise(pt_divs = median(divs_from_mrca, na.rm = TRUE)) %>%
    left_join(clinical_tbl) %>%
    mutate(msi=ifelse(subject %in% msi_tumors, TRUE, FALSE)) %>% 
    group_by(msi) %>% 
    mutate(
        volume = (pi*size^3)/6, cell_count = volume * 1e9, growth_rate = cell_count^(1 / pt_divs),
        death_rate=1-(growth_rate-1), death_birth_ratio=death_rate/1, test=2-death_rate
    ) %>% 
    summarize(median(death_rate), median(growth_rate))

Joining with `by = join_by(subject)`

A tibble: 2 x 3

msi	median(death_rate)	median(growth_rate)
<lgl>	<dbl>	<dbl>
FALSE	0.9695792	1.030421
TRUE	0.9701420	1.029858

Numbers for the text

Number of MMRd and MMRp samples

msi_samples <- markerlengths %>%
    group_by(subject) %>%
    mutate(large_del = (length < (-1))) %>%
    count(large_del) %>%
    mutate(del_frac = n / sum(n)) %>%
    filter(large_del, del_frac > 0.1)
msi_samples %>%
    nrow()
37 - 6

6

31

Sample numbers for first paragraph:

# all samples
n_distinct(c(l1_tbl %>%
    pull(a), l1_tbl %>%
    pull(b)))

505

sample_number <- function(type) {
    n_distinct(c(l1_tbl %>%
    pull(a), l1_tbl %>%
    pull(b)) %>% 
        str_subset(type)
    )
}

#normal samples
sample_number("N")

73

#adenomas
sample_number("Ad")

17

#primary tumor
sample_number("P")

183

#LN mets
sample_number("L")

130

#distant mets
sample_number("M")

102

# tumor samples
sample_number("Ad") + sample_number("P")+sample_number("L")+sample_number("M")

432

Cell divisions to cancer MRCA

mrca_tbl %>%
    filter(!(subject %in% msi_tumors)) %>%
    summarise(median(all_mrca), sd(all_mrca))

A tibble: 1 x 2

median(all_mrca)	sd(all_mrca)
<dbl>	<dbl>
1347.414	639.5609

Cell divisions to adenoma MRCA

mrca_tbl %>%
    summarise(median(ad_ad_mrca, na.rm = T), sd(ad_ad_mrca, na.rm = T))

A tibble: 1 x 2

median(ad_ad_mrca, na.rm = T)	sd(ad_ad_mrca, na.rm = T)
<dbl>	<dbl>
906.2799	483.6381

ISC donor ages

min(c(4, 4, 9, 14, 66))
max(c(4, 4, 9, 14, 66))

4

66

Divisions since tumor MRCA per sample type. Only synchronous distant metastases.

plot_divs_from_mrca %>%
    group_by(sample_type) %>%
    filter(!is.na(divs_from_mrca)) %>% 
    summarise(median(divs_from_mrca, na.rm = TRUE), sd(divs_from_mrca, na.rm = TRUE), count=n())

A tibble: 4 x 4

sample_type	median(divs_from_mrca, na.rm = TRUE)	sd(divs_from_mrca, na.rm = TRUE)	count
<fct>	<dbl>	<dbl>	<int>
A	631.6603	502.4743	13
P	811.3547	691.2512	183
L	1012.7399	703.4256	130
M	1421.4491	748.3837	69

Divergence and diversification timing from cancer MRCA

patient_mrca %>%
    select(-comparison) %>%
    left_join(divergence_timing) %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    mutate(mrca = mrca - divs) %>%
    group_by(comparison, subject) %>%
    summarise(divs = median(mrca)) %>% 
    summarise(median(divs, na.rm=T), sd=sd(divs, na.rm=T))

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'comparison'. You can override using the
`.groups` argument.

A tibble: 5 x 3

comparison	median(divs, na.rm = T)	sd
<chr>	<dbl>	<dbl>
adenoma_adenoma	-128.6973	430.5136
ln_primary	372.1827	498.2519
met_primary	507.3118	534.7928
primary_primary	252.2611	449.4946
NA	NA	NA

Patients with metastasis divergence before primary tumor diversification.

met_divg_class <- patient_mrca %>%
    select(-comparison) %>%
    left_join(divergence_timing) %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    filter(comparison != "adenoma_adenoma") %>%
    mutate(mrca = mrca - divs) %>%
    group_by(comparison, subject) %>%
    summarize(mrca = median(mrca)) %>%
    ungroup() %>%
    mutate(comparison = fct_relevel(
        comparison,
        "primary_primary", "ln_primary", "met_primary"
    )) %>%
    group_by(subject) %>%
        filter(comparison != "ln_primary") %>%
        filter(n() == 2) %>%
        mutate(mrca = mrca - mrca[comparison == "primary_primary"])
    

# early divergence
met_divg_class %>%
    filter(mrca < 0, comparison == "met_primary") %>%
    nrow()
# late divergence
met_divg_class %>%
    filter(mrca >= 0,  comparison=="met_primary") %>%
    nrow()

Joining with `by = join_by(subject)`
`summarise()` has grouped output by 'comparison'. You can override using the
`.groups` argument.

2

24

24/26*100

92.3076923076923

Division times of metastases seeding primary tumor regions:

Numbers for last paragraph of section for Fig 3

pt_mrca_ln_met_divg <- divergence_timing %>%
    mutate(comparison = ifelse(str_detect(samples, "L"), "ln_primary", comparison)) %>%
    group_by(subject, comparison) %>%
    summarize(divs = median(mrca))

# divs from zygote to sample type
divs_to_sample <- annotated_cmb_cell_divs %>%
    filter((str_detect(a, "N") & !str_detect(b, "N")) | (str_detect(b, "N") & !str_detect(a, "N"))) %>%
    mutate(comparison = ifelse(type_a == "N", type_b, type_a)) %>%
    select(subject, comparison, divs) %>% 
    group_by(subject, comparison) %>%
    summarize(divs = median(divs))

`summarise()` has grouped output by 'subject'. You can override using the
`.groups` argument.
`summarise()` has grouped output by 'subject'. You can override using the
`.groups` argument.

bind_rows(median_mrca_tbl, divg_med_tbl, divs_to_sample_med_tbl) %>%
    mutate(divs = ifelse(comparison != "all_mrca", divs + divs[comparison == "all_mrca"], divs))

A tibble: 8 x 2

comparison	divs
<chr>	<dbl>
all_mrca	1347.414
ln_primary	1719.596
met_primary	1854.725
primary_primary	1599.675
A	NA
P	2158.768
L	2360.153
M	2768.863

Total number of cell divisions across all samples.

annotated_cmb_cell_divs %>%
    filter((str_detect(a, "N") & !str_detect(b, "N")) | (str_detect(b, "N") & !str_detect(a, "N"))) %>%
    mutate(comparison = ifelse(type_a == "N", type_b, type_a)) %>%
    filter(comparison!="A") %>% 
    ungroup() %>% 
    summarise(divs = median(divs))

A tibble: 1 x 1

divs
<dbl>
2559.46

Number of PT regions per subject

plot_divs_from_mrca %>%
    filter(sample_type=="P") %>% 
    count(subject) %>% 
    summarise(mean(n))

A tibble: 1 x 1

mean(n)
<dbl>
4.945946

Sample number in Hu et al

hu_sheets <- excel_sheets("../data/hu_2019_supplement.xlsx")

pt_samples_in_hu <- function(sheet) {
    read_excel("../data/hu_2019_supplement.xlsx", sheet = sheet) %>%
        select(ends_with("_cover") & contains("P")) %>%
        ncol()
}

pt_n_list <- lapply(hu_sheets, pt_samples_in_hu)

pt_n_list %>%
    unlist() %>%
    length()

23

pt_n_list %>%
    unlist() %>%
    mean()

2.39130434782609

Mutation burden in polyGs in Hu/Curtis data

plot_divs_from_mrca %>%
    group_by(sample_type) %>%
    summarise(divs=median(divs_from_mrca, na.rm = TRUE), sd(divs_from_mrca, na.rm = TRUE)) %>%
    ungroup() %>%
    mutate(divs=divs/divs[sample_type=="P"])

A tibble: 4 x 3

sample_type	divs	sd(divs_from_mrca, na.rm = TRUE)
<fct>	<dbl>	<dbl>
A	0.7785255	502.4743
P	1.0000000	691.2512
L	1.2482087	703.4256
M	1.7519455	748.3837

hu_mb <- read_excel("../data/mutation_burden/Hu_Curtis_mutations_mets_PT.xlsx")

hu_mb %>%
    summarise(burden_diff = mean(m_clonal_mut_burden)/mean(p_clonal_mut_burden))

A tibble: 1 x 1

burden_diff
<dbl>
1.197095

C66 division burden

tumor_ad_mrca %>%
       left_join(annotated_cmb_cell_divs) %>%
    group_by(subject) %>%
    filter((str_detect(a, "N") | str_detect(b, "N"))) %>%
    ungroup() %>%
    mutate(
           divs_from_mrca = ifelse(str_detect(a, "A") | str_detect(b, "A"), divs - ad_divs, divs - mrca_divs),
           sample_type = ifelse(type_a == "N", type_b, type_a)
    ) %>%
    mutate(sample_type = fct_relevel(sample_type, "A", "P", "L", "M")) %>%
        filter(subject == "C66") %>%
        group_by(sample_type) %>%
        summarise(mean(divs_from_mrca))

Joining with `by = join_by(subject)`

A tibble: 3 x 2

sample_type	mean(divs_from_mrca)
<fct>	<dbl>
P	696.1494
L	670.6022
M	1276.1634

1276.1634/670.6022

1.90301105483996